Department of Molecular and Cellular Physiology, Stanford University, Stanford, CA 94305, USA.
Neuron. 2010 Nov 18;68(4):639-53. doi: 10.1016/j.neuron.2010.09.024.
A lack of methods for measuring the protein compositions of individual synapses in situ has so far hindered the exploration and exploitation of synapse molecular diversity. Here, we describe the use of array tomography, a new high-resolution proteomic imaging method, to determine the composition of glutamate and GABA synapses in somatosensory cortex of Line-H-YFP Thy-1 transgenic mice. We find that virtually all synapses are recognized by antibodies to the presynaptic phosphoprotein synapsin I, while antibodies to 16 other synaptic proteins discriminate among 4 subtypes of glutamatergic synapses and GABAergic synapses. Cell-specific YFP expression in the YFP-H mouse line allows synapses to be assigned to specific presynaptic and postsynaptic partners and reveals that a subpopulation of spines on layer 5 pyramidal cells receives both VGluT1-subtype glutamatergic and GABAergic synaptic inputs. These results establish a means for the high-throughput acquisition of proteomic data from individual cortical synapses in situ.
目前缺乏在原位测量单个突触蛋白组成的方法,这一直阻碍了对突触分子多样性的探索和开发。在这里,我们描述了使用阵列断层扫描(array tomography),一种新的高分辨率蛋白质组学成像方法,来确定 Line-H-YFP Thy-1 转基因小鼠体感皮层中谷氨酸能和 GABA 能突触的组成。我们发现,几乎所有的突触都可以被突触前磷酸蛋白突触素 I 的抗体识别,而 16 种其他突触蛋白的抗体可以区分 4 种谷氨酸能突触和 GABA 能突触亚型。YFP-H 小鼠系中的细胞特异性 YFP 表达允许将突触分配给特定的突触前和突触后伙伴,并揭示了 5 层锥体神经元上的一个亚群棘突同时接收 VGluT1 型谷氨酸能和 GABA 能突触输入。这些结果为高通量获取原位单个皮质突触的蛋白质组学数据建立了一种方法。